CAS 28772-56-7
:2H-1-Benzopyran-2-one, 3-[3-(4′-bromo[1,1′-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-
Description:
The chemical substance known as 2H-1-Benzopyran-2-one, 3-[3-(4′-bromo[1,1′-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy- is a complex organic compound characterized by its polycyclic structure, which includes a benzopyran moiety. This compound features multiple functional groups, including hydroxyl (-OH) groups and a bromo-substituted biphenyl, contributing to its potential reactivity and biological activity. The presence of the benzopyran structure suggests that it may exhibit properties typical of flavonoids, such as antioxidant activity. The bromo substituent can enhance lipophilicity and influence the compound's interaction with biological targets. Additionally, the compound's intricate structure may allow for various stereochemical configurations, which can affect its pharmacological properties. Overall, this substance may be of interest in medicinal chemistry and pharmacology, particularly in the development of therapeutic agents. However, specific properties such as solubility, melting point, and biological activity would require empirical investigation for comprehensive understanding.
Formula:C30H23BrO4
InChI:InChI=1S/C30H23BrO4/c31-23-16-14-20(15-17-23)19-10-12-22(13-11-19)26(32)18-25(21-6-2-1-3-7-21)28-29(33)24-8-4-5-9-27(24)35-30(28)34/h1-17,25-26,32-33H,18H2
InChI key:InChIKey=OWNRRUFOJXFKCU-UHFFFAOYSA-N
SMILES:C(CC(O)C1=CC=C(C=C1)C2=CC=C(Br)C=C2)(C3=C(O)C=4C(OC3=O)=CC=CC4)C5=CC=CC=C5
Synonyms:- 2H-1-Benzopyran-2-one, 3-[3-(4′-bromo[1,1′-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-
- 3-[3-(4'-bromobiphenyl-4-yl)-3-hydroxy-1-phenylpropyl]-2-hydroxy-4H-chromen-4-one
- 3-[3-(4'-bromobiphenyl-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-2H-chromen-2-one
- 3-[3-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-hydroxy-1-phenylpropyl]-4-hydroxy-2H-1-benzopyran-2-one
- Bromadiolone
- Coumarin, 3-[α-[p-(p-bromophenyl)-β-hydroxyphenethyl]benzyl]-4-hydroxy-
- Hemus AB
- Ratonil
- Roban
- Maki
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Found 8 products.
Bromadiolone (Mixture of Diastereomers)
CAS:Formula:C30H23BrO4Color and Shape:White To Off-White SolidMolecular weight:527.41Rodenticides Mixture 248 100 µg/mL in Acetonitrile
CAS:Controlled ProductFormula:C31H23BrO3Color and Shape:MixtureMolecular weight:523.42Bromadiolone-d5 (Mixture of Diasteromers)
CAS:Controlled ProductFormula:C30D5H18BrO4Color and Shape:NeatMolecular weight:532.44Bromadiolone
CAS:Controlled Product<p>Applications Bromadiolone is an anticoagulant rodenticide used on non-crop areas.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Cherry, L., et al.: Toxicologist, 2, 108 (1992), Park, B., et al.: Biochem. Pharmacol., 31, 3635 (1992), Thijssen, H., et al.: Pestic Sci., 43, 73 (1995), Howald, G., et al.: Conserv. Biol., 21, 1258 (2007),<br></p>Formula:C30H23BrO4Color and Shape:WhiteMolecular weight:527.41Bromadiolone
CAS:<p>Bromadiolone NA is a rodenticide that is used in the treatment of rodents in wastewater treatment. Bromadiolone NA has been shown to inhibit the mitochondrial membrane potential, which leads to the release of cytochrome C and activation of caspase 3. Bromadiolone NA also has antioxidative properties that protect against oxidative injury and its metabolites have been found to inhibit human serum albumin. This compound has been used as an antimicrobial agent to control biofilm formation and prevent microbial growth. The mode of action for bromadiolone is through the inhibition of chitosan polymerization, which prevents bacterial attachment and biofilm formation on surfaces. Bromadiolone NA was also shown to bind with DNA, inhibiting replication and transcription.</p>Formula:C30H23BrO4Purity:Min. 95%Color and Shape:PowderMolecular weight:527.41 g/mol





